Structure of PDB 2gvf Chain A Binding Site BS02
Receptor Information
>2gvf Chain A (length=183) [
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MGAPITAYAQQTRGLLGCIITSLTGRDKNQVEGEVQIVSTATQTFLATCI
NGVCWTVYHGAGTRTIASPKGPVIQMYTNVDQDLVGWPAPQGSRSLTPCT
CGSSDLYLVTRHADVIPVRRRGDSRGSLLSPRPISYLKGSSGGPLLCPAG
HAVGLFRAAVCTRGVAKAVDFIPVENLETTMRS
Ligand information
>2gvf Chain D (length=16) Species:
11104
(Hepatitis C virus (isolate 1)) [
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GSVVIVGRIVLSGKPA
Receptor-Ligand Complex Structure
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PDB
2gvf
P2-P4 macrocyclic inhibitors of hepatitis C virus NS3-4A serine protease.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
T4 A5 Y6 A7
Binding residue
(residue number reindexed from 1)
T6 A7 Y8 A9
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D81 G137 S139
Catalytic site (residue number reindexed from 1)
H59 D83 G139 S141
Enzyme Commision number
2.7.7.48
: RNA-directed RNA polymerase.
3.4.21.98
: hepacivirin.
3.4.22.-
3.6.1.15
: nucleoside-triphosphate phosphatase.
3.6.4.13
: RNA helicase.
Gene Ontology
Molecular Function
GO:0008236
serine-type peptidase activity
Biological Process
GO:0006508
proteolysis
GO:0019087
transformation of host cell by virus
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Molecular Function
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Biological Process
External links
PDB
RCSB:2gvf
,
PDBe:2gvf
,
PDBj:2gvf
PDBsum
2gvf
PubMed
16730985
UniProt
P26664
|POLG_HCV1 Genome polyprotein
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